Variant report

Variant	rs7305222
Chromosome Location	chr12:10203544-10203545
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10505749	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1074059	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1074060	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10845026	0.89[EUR][1000 genomes]
rs10845028	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1488818	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4399401	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6488246	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7132536	0.83[EUR][1000 genomes]
rs7297150	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7315231	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7972323	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10195400-10203800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr12:10201800-10204200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr12:10201800-10204200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr12:10202000-10203800	Weak transcription	Primary monocytes fromperipheralblood	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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